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443776-76-9

443776-76-9 Structure

443776-76-9 Structure
IdentificationBack Directory
[Name]

(3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)methanol
[CAS]

443776-76-9
[Synonyms]

3-Hydroxymethylphenylboronic acid, pinacol ester
3-(Hydroxymethyl)benzeneboronicacid,pinacolester96%
3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl Alcohol
3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzenemethanol
2-(3-Hydroxymethylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
Benzenemethanol, 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
[Molecular Formula]

C13H19BO3
[MDL Number]

MFCD09266196
[MOL File]

443776-76-9.mol
[Molecular Weight]

234.11
Chemical PropertiesBack Directory
[Melting point ]

42-46 °C
[Boiling point ]

363.7±25.0 °C(Predicted)
[density ]

1.07±0.1 g/cm3(Predicted)
[Fp ]

110 °C
[storage temp. ]

2-8°C
[form ]

powder to lump
[pka]

14.34±0.10(Predicted)
[color ]

White to Almost white
[InChI]

InChI=1S/C13H19BO3/c1-12(2)13(3,4)17-14(16-12)11-7-5-6-10(8-11)9-15/h5-8,15H,9H2,1-4H3
[InChIKey]

ZEWWJJQAFTXUIS-UHFFFAOYSA-N
[SMILES]

C1(CO)=CC=CC(B2OC(C)(C)C(C)(C)O2)=C1
Questions And AnswerBack Directory
[Uses]

Pinaryl 3-hydroxymethylphenylboronic acid can be used as a pharmaceutical synthesis intermediate.
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[WGK Germany ]

3
[HS Code ]

2931900090
[Storage Class]

13 - Non Combustible Solids
Spectrum DetailBack Directory
[Spectrum Detail]

(3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)methanol(443776-76-9)1HNMR
Hazard InformationBack Directory
[Synthesis]

3-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)-BENZALDEHYDE

380151-86-0

(3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)methanol

443776-76-9

GENERAL METHOD: Methanol (12.50 mL) was added to a mixture of 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde (1a, 375 mg, 2.50 mmol), pinacol (355 mg, 3.00 mmol) and anhydrous magnesium sulfate (625 mg, 5.00 mmol). The mixture was stirred at room temperature for 6 hours. Upon completion of the reaction, the crude reaction mixture was filtered and then sodium borohydride (47 mg, 1.25 mmol) was added to the filtrate. Subsequently, the reaction mixture was stirred for another 5 hours. After completion of the reaction, the reaction mixture was filtered and the filtrate was concentrated in vacuum to afford the target product 3-hydroxymethylphenylboronic acid pinacol ester (2a) as a white solid (melting point 75-77 °C) in 88% yield (513 mg).1H-NMR (CD3OD-d4) δ ppm: 7.71 (d, J=8.0 Hz, 2H), 7.35 (d, J=7.8 Hz. 2H), 4.62 (s, 2H), 1.34 (s, 12H); 13C-NMR (CD3OD-d4) δppm: 146.23, 135.93, 127.26, 85.19, 65.24, 25.34; 11B-NMR (CDCl3) δppm: 34.82.

[References]

[1] Molecules, 2013, vol. 18, # 10, p. 12346 - 12367
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